US Pharmacia sp. z o.o.
US Pharmacia ist ein polnischer Hersteller von dermatologischen und ophthalmologischen Präparaten, produziert…
US Pharmacia ist ein polnischer Hersteller von dermatologischen und ophthalmologischen Präparaten, der Magistral- und Industriepharmazeutika herstellt, darunter Augentropfen, topische Cremes, orale Lösungen und zusammengesetzte Apothekenbestandteile. Das Unternehmen beliefert Krankenhausapotheken, Einzelhandelsapotheken und dermatologische Spezialkliniken in ganz Polen mit lizenzierten pharmazeutischen Spezialitäten und stellt einige Produkte im Auftrag europäischer Pharmahändler her.
- Type
- brand seeking distribution
- Location
- Wrocław, Poland
- Founded
- 1990
- Website
- uspharmacia.pl
- Categories
- Medizin- & Gesundheitsbedarf, Hautpflege & Kosmetik
- Markets
- Polen, Tschechien, Slowakei, Ungarn, Rumänien, Deutschland, Litauen
Verified facts
- vat-valid (green), checked 2026-08-01 VIES (European Commission)
- registered-units (green), checked 2026-08-21 REGON national business register (GUS, Poland)
- registry-activity (green), checked 2026-08-21 REGON national business register (GUS, Poland)
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- domain-registered (green), checked 2026-08-13 Domain registry record
- registered-address (green), checked 2026-08-20 Ministry of Finance VAT white list (Poland)
- registered-since (green), checked 1996-09-16 Ministry of Finance VAT white list (Poland)
- tax-filing-active (green), checked 2026-08-20 Ministry of Finance VAT white list (Poland)
- gmp-certified (green), checked 2023-10-20 EudraGMDP, EU register of GMP certificates (EMA)
- operating-permit (green), checked 2026-08-19 EudraGMDP manufacturing authorisation register (EMA)
Claimed certifications
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
Import rules for these goods
- Cosmetic products must be notified in the EU Cosmetic Products Notification Portal (CPNP) before being placed on the EU market. European Commission (CPNP)
- For the US market, MoCRA requires cosmetic facility registration and product listing with the FDA. US FDA (MoCRA)
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)